NDC 73581-027 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC73581-027
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- YYBA Corp
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA210137
- Marketed since
- October 1, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 180 mg/1
Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 73581-027-01 | 10 TABLET in 1 BOTTLE (73581-027-01) | Oct 3, 2025 |
| 73581-027-04 | 40 TABLET in 1 BOTTLE (73581-027-04) | Oct 3, 2024 |
| 73581-027-10 | 100 TABLET in 1 BOTTLE (73581-027-10) | Oct 3, 2025 |
| 73581-027-20 | 200 TABLET in 1 BOTTLE (73581-027-20) | Oct 29, 2025 |
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